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Project Engineer Medical Device Jobs in Philadelphia, PA

The Project Engineer will be responsible for all engineering functions of their product lines. This ... Medical device experience strongly preferred * Bachelor's Degree in Mechanical Engineering ...

PROJECT ENGINEER We are seeking a dynamic and detail-oriented Project Engineer to join our Product ... medical device experience strongly preferred. * Endovascular product design experience preferred.

PROJECT ENGINEER We are seeking a dynamic and detail-oriented Project Engineer to join our Product ... medical device experience strongly preferred. * Endovascular product design experience preferred.

The Project Engineer will be responsible for all engineering functions of their product lines. This ... Medical device experience strongly preferred * Bachelor's Degree in Mechanical Engineering ...

Medical device experience strongly preferred • Bachelor's Degree in Mechanical Engineering ... project budgets • Strong knowledge of Microsoft Office • Ability to attend surgeries and/or ...

PROJECT ENGINEER We are seeking a dynamic and detail-oriented Project Engineer to join our Product ... medical device experience strongly preferred. * Endovascular product design experience preferred.

PROJECT ENGINEER We are seeking a dynamic and detail-oriented Project Engineer to join our Product ... medical device experience strongly preferred. * Endovascular product design experience preferred.

The Project Engineer will be responsible for all engineering functions of their product lines. This ... Medical device experience strongly preferred * Bachelor's Degree in Mechanical Engineering ...

The Project Engineer will be responsible for all engineering functions of their product lines. This ... Medical device experience strongly preferred * Bachelor's Degree in Mechanical Engineering ...

Medical device experience strongly preferred Bachelor's Degree in Mechanical Engineering ... project budgets Strong knowledge of Microsoft Office Ability to attend surgeries and/or labs Our ...

Create and maintain project plans and FDA-compliant Design History Files (DHF) for each project ... medical device experience strongly preferred. * Proficiency in CREO and/or SolidWorks software for ...

Create and maintain project plans and FDA-compliant Design History Files (DHF) for each project ... medical device experience strongly preferred. * Proficiency in CREO and/or SolidWorks software for ...

Creating and maintaining project plans and FDA complaint Design history Files (DHF) for each ... Medical device experience strongly preferred * Bachelor's Degree in Mechanical Engineering ...

Creates and maintains project plans and FDA complaint Design history Files (DHF) for each project ... Medical device experience strongly preferred * Bachelor's Degree in Mechanical Engineering ...

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Showing results 1-20

Project Engineer Medical Device information

See Philadelphia, PA salary details

$45.4K

$91.5K

$137.2K

How much do project engineer medical device jobs pay per year?

As of Aug 15, 2026, the average yearly pay for project engineer medical device in Philadelphia, PA is $91,467.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,700.00 and $104,400.00 per year, depending on experience, location, and employer.

What does a project engineer do in the medical device industry?

A Project Engineer in the medical device industry is responsible for planning, coordinating, and managing projects related to the development and manufacturing of medical devices. They oversee project timelines, budgets, and resources, ensuring that all technical and regulatory requirements are met. Their work involves collaborating with cross-functional teams, such as design, quality assurance, and regulatory affairs, to bring safe and effective medical devices to market. Project Engineers also help resolve technical challenges and ensure products comply with industry standards and government regulations.

How does a project engineer in the medical device industry typically collaborate with cross-functional teams during product development?

As a Project Engineer in the medical device field, you’ll work closely with cross-functional teams such as R&D, quality assurance, regulatory affairs, and manufacturing. Collaboration involves coordinating project timelines, ensuring design requirements are met, and facilitating communication between departments to address technical challenges and regulatory compliance. Regular meetings and clear documentation are essential to keep all stakeholders aligned, and you may often serve as a bridge between engineering and non-engineering teams. This collaborative environment fosters innovation and helps ensure the successful and timely launch of safe, effective medical devices.

What is the difference between Project Engineer Medical Device vs Quality Engineer Medical Device?

AspectProject Engineer Medical DeviceQuality Engineer Medical Device
Required CredentialsBachelor's in Engineering, certifications like PMP beneficialBachelor's in Engineering or Science, certifications like CQE preferred
Work EnvironmentDesign, development, and project management teams in manufacturing or R&DQuality assurance, compliance, and inspection teams in manufacturing
Employer & Industry UsageMedical device companies focusing on product development and project executionMedical device companies ensuring product quality and regulatory compliance
Common Search & Comparison IntentUnderstanding project management roles in medical device industryUnderstanding quality assurance roles in medical device industry

The Project Engineer Medical Device focuses on managing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Quality Engineer Medical Device concentrates on maintaining product quality, compliance with regulations, and conducting inspections. Both roles are essential in medical device companies but serve different functions within the product lifecycle.

What are the key skills and qualifications needed to thrive as a project engineer in the medical device industry?

To excel as a Project Engineer in medical devices, you need a solid background in engineering (typically a degree in biomedical, mechanical, or electrical engineering), experience with product development, and knowledge of regulatory standards like FDA and ISO 13485. Familiarity with CAD software, project management tools, and validation protocols is highly valuable, along with certifications such as PMP or Six Sigma. Strong problem-solving abilities, collaboration, and effective communication are essential soft skills for leading cross-functional teams and resolving technical challenges. These skills and qualifications ensure safe, compliant, and innovative device development that meets patient and market needs.

What job categories do people searching Project Engineer Medical Device jobs in Philadelphia, PA look for?

The top searched job categories for Project Engineer Medical Device jobs in Philadelphia, PA are:

Infographic showing various Project Engineer Medical Device job openings in Philadelphia, PA as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 18% Part Time, 1% Temporary, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $91,467 per year, or $44 per hour.

Senior Project Engineer - Acute Care

Boehringer Laboratories Inc

Phoenixville, PA • On-site

$99K - $130K/yr

Full-time

Retirement

Re-posted 21 days ago


Job description

Senior Project Engineer - Acute Care

Our exciting growth has identified the need to add a Senior Project Engineer to join our Acute Care Commercialization team! The ideal candidate is an individual that has a passion for innovation while supporting a variety of engineering initiatives in the medical device industry.

Overview of the Role

The Senior Project Engineer is responsible for planning and coordinating engineering initiatives to support existing products and new product development. This includes researching regulations, developing project implementation plans, generating specifications, and managing allocated resources to ensure project success.

Who You’ll Work With

You will report to the Acute Care Engineering Manager while working closely with the entire Acute Care Commercialization team to support new and existing product initiatives. Cross functional collaboration between Operations, Finance, and Sales are integrated throughout the product development process.

Major Accountabilities

  • Lead full product ideation, feasibility, and design activities, incorporating clinical feedback and market research across the life cycle of new product development and existing product support.
  • Develop project objectives, scope, and timelines in collaboration with leadership.
  • Work closely with cross-functional teams (quality, manufacturing, marketing, clinical, and sales) to hit milestones on time and within budget.
  • Initiate technical and design decisions that balance clinical needs, manufacturability, cost, and regulatory pathway.

Duties and Responsibilities

  • Author and maintain project documentation, including project plans, SOPs, work instructions, and Design History Files (DHF).
  • Author regulatory clearance submissions (FDA 510(k), CE Mark, etc.) ensuring minimum requirements are met.
  • Contribute to IP strategy, work with patent attorneys to identify and protect novel innovations.
  • Research regulations and ensure compliance with FDA design control requirements.
  • Support project launches and implementation of post-market design improvements.
  • Identify and resolve production scale-up challenges; transition designs from development to manufacturing and commercialization.
  • Conduct process and equipment validation activities; support packaging and labeling validations.
  • Engage clinicians to identify unmet needs through direct clinical observation in the hospital environment (operating room, ICU, etc.).
  • Assist with supplier qualification, audits, and quality performance feedback.
  • Continuously improve quality systems, processes, documentation and assist with quality audits.

Qualifications

  • A bachelor’s degree in mechanical or biomedical engineering is required.
  • Minimum of 8 years of mechanical and/or technical experience working in the medical device field.
  • Proficiency in CAD software for design and drafting (SolidWorks).
  • Ability to plan, organize, and execute complex projects within a timeline and a budget.
  • Excellent problem-solving skills with experience in root cause analysis and risk management.
  • Strong communication skills, interacting effectively with clinicians, management, and cross-functional teams.
  • Strong knowledge of FDA regulations, ISO 13485, and medical device quality systems.

Who We Are & What We Do

Boehringer Laboratories, LLC is a US based Medica Device Manufacturer headquartered in Phoenixville, PA. We serve the Acute Care Hospital Market in the US and across the Globe. We have strong product lines in the Minimally Invasive Surgery and Medical Gas spaces. We continually strive to grow as a company by creating novel devices that improve patient care.

We seek to make world-class products that improve patients’ lives. We are dedicated to improving our skills to serve our customers, community, and each other. We are a team of professionals passionate in our work. Our Mission: Caring for Lives through Innovation, Quality, and Service. To learn more about our company, visit www.boehringerlabs.com .

We provide an environment that fosters professional growth while offering an excellent wage and benefits package, including a 401(k) with employer match.